blue fluorescence
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RSC Advances ◽  
2022 ◽  
Vol 12 (3) ◽  
pp. 1352-1360
Author(s):  
Karan Surana ◽  
R. M. Mehra ◽  
Saurabh S. Soni ◽  
Bhaskar Bhattacharya

Carbon QD showing bright blue fluorescence aid in improving the photovoltaic parameters in a co-sensitized solar cell. Time-dependent I–V analysis revealed the real-time functioning of the device.


Author(s):  
Ina Nur Istiqomah ◽  
Hanif Mubarok ◽  
Taehwan Lee ◽  
Ngoc Tuyet Nhi Nguyen ◽  
Jaehoon Jung ◽  
...  
Keyword(s):  

Optik ◽  
2021 ◽  
pp. 168517
Author(s):  
Xuying Feng ◽  
Yuhang Sheng ◽  
Ming Meng ◽  
Jinlei Zhang ◽  
Shuyi Wu ◽  
...  

2021 ◽  
Author(s):  
Rentian Guan ◽  
Shuai Zhang ◽  
Xiaoyu Fan ◽  
Xiaodong Shao ◽  
Yingying Hu ◽  
...  

Abstract It was the first time to report the aggregation induced emission (AIE) of acetaldehyde (AA) on the surface of carbonized polymer dots (CPDs) with the auxiliary of Tb3+. Based on the AIE of AA, a turn-off-on fluorescence method was established for AA detection using the porous CPDs-Tb3+ system. The one-pot hydrothermal method was used to obtain CPDs, using milk and polyethyleneimine (PEI) as precursors. In the presence of Tb3+, CPDs aggregated immediately, and the fluorescence intensity decreased obviously for the precipitate. AA can effectively embed on the surface of CPDs-Tb3+ due to the porous structure. AA displayed obviously blue fluorescence with excitation wavelength at 370 nm (emission peak at 460 nm), while there was no fluorescence peak when excited at 460 nm. In the CPDs-Tb3+ solution, AA exhibits obvious fluorescence enhancement effect (lex 460 nm, lem 545 nm). And then, AA can be determined by the turn-off-on system based on the linear relationship between fluorescence enhancement and the concentration of AA ranging from 0.04 mM to 42.48 mM. The limit of detection (LOD) was 0.02 mM. The turn-off-on system was successfully applied to determine AA in wine samples. The strategy may be exploited to monitor AA in more drinking or foodstuff samples.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Alessio Terenzi ◽  
Mery La Franca ◽  
Sushilla van Schoonhoven ◽  
Rostyslav Panchuk ◽  
Álvaro Martínez ◽  
...  

AbstractLandomycins are angucyclines with promising antineoplastic activity produced by Streptomyces bacteria. The aglycone landomycinone is the distinctive core, while the oligosaccharide chain differs within derivatives. Herein, we report that landomycins spontaneously form Michael adducts with biothiols, including reduced cysteine and glutathione, both cell-free or intracellularly involving the benz[a]anthraquinone moiety of landomycinone. While landomycins generally do not display emissive properties, the respective Michael adducts exerted intense blue fluorescence in a glycosidic chain-dependent manner. This allowed label-free tracking of the short-lived nature of the mono-SH-adduct followed by oxygen-dependent evolution with addition of another SH-group. Accordingly, hypoxia distinctly stabilized the fluorescent mono-adduct. While extracellular adduct formation completely blocked the cytotoxic activity of landomycins, intracellularly it led to massively decreased reduced glutathione levels. Accordingly, landomycin E strongly synergized with glutathione-depleting agents like menadione but exerted reduced activity under hypoxia. Summarizing, landomycins represent natural glutathione-depleting agents and fluorescence probes for intracellular anthraquinone-based angucycline metabolism.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6894
Author(s):  
Natalia L. Zaichenko ◽  
Tatyana M. Valova ◽  
Olga V. Venidiktova ◽  
Alexander V. Lyubimov ◽  
Andrey I. Shienok ◽  
...  

Spectral-luminescence properties of a hybrid compound containing a coumarin-type spiropyran and an azomethinocoumarin fragment in toluene-acetonitrile solution in the presence of Li+, Ca2+, Zn2+ and Mg2+ ions are reported. Two excited state proton transfers can occur in the hybrid compound—the transfer of a proton from the OH group of the 7-hydroxy coumarin tautomer to the N atom of the C=N bond of the azomethine fragment leading to green ESIPT fluorescence with a maximum at 540 nm and from the OH group of the 7-hydroxy coumarin tautomer to the carbonyl group of the pyrone chromophore, which leads to the formation of the 2-hydroxyl-tautomer T of coumarin with blue fluorescence with a maximum at 475 nm. Dependence of these excited state proton transfers on the metal nature and irradiation with an external UV source is discussed.


2021 ◽  
Author(s):  
◽  
Ying Tang

<p>The lignocellulosic fibres extracted from the leaves of New Zealand flax, Phormium tenax, have been used as the principal textile fibre by Maori since pre- European times. Variations of antifungal activity were observed in Phormium fibres of different cultivars. The most resistant cultivars of P. tenax in an aqueous antifungal assay also possessed the greatest variety of naturally-occurring 7-hydroxycoumarins as identified by mass spectroscopy, ESI-MS. In addition to antifungal effects, coumarins function as fluorescent whitening agents in Phormium fibres and play a role in the fibre’s photodegradation. Ultraviolet irradiation (350 – 400 nm) of the fibre resulted in a substantial loss of the blue fluorescence originating from a number of 7-hydroxycoumarins present, together with the formation of new fluorophores absorbing and emitting at longer wavelengths, which contribute to the photoyellowing of the fibre. The photolysis of two standard 7-hydroxycoumarins in aqueous solution was examined and two primary photoproducts were elucidated by ESI-MS: a photodimer containing a linking cyclobutane ring and a monomeric photooxidation product. The formation of at least some of the photoproducts is associated with the coumarin-sensitised generation of reactive oxygen species, hydrogen peroxide and superoxide. The fluorescence properties and photodegradation of Chinese handmade papers were also investigated. Papers manufactured by traditional methods were found to be more photostable than that produced from chemically-facilitated techniques.</p>


2021 ◽  
Author(s):  
Elham Rashidi Rashidi ◽  
Neda Esfandiari ◽  
Zahra Ranjbar ◽  
Nikta Alvandi ◽  
Zahra Fatahi

Abstract During recent years, cancer has been recognized as a well-known disorder all over the world. One of the important factors to tackle this problem better than past decades is early diagnosis that takes into practice by state-of-the-art visual equipment for detection cancer cells. Herein, in this research, we synthesized carbon dots with pH-dependent behavior from a green source by hydrothermal method with high quantum yield and blue fluorescence. Folic acid-conjugated carbon dots by an efficient and optimal conjugation method were set upped which determined cancer cells visually. These synthesized and conjugated nanoparticles entered into the cancer cells more comprehensive than normal cells by receptor-mediated endocytosis and could distinguish cancer cells from normal ones by fluorescence imaging. Ultimately, synthesized nanoparticles in this research can be considered as an efficient fluorescent nanoprobe for cancer pre-diagnosis.


2021 ◽  
Author(s):  
◽  
Ying Tang

<p>The lignocellulosic fibres extracted from the leaves of New Zealand flax, Phormium tenax, have been used as the principal textile fibre by Maori since pre- European times. Variations of antifungal activity were observed in Phormium fibres of different cultivars. The most resistant cultivars of P. tenax in an aqueous antifungal assay also possessed the greatest variety of naturally-occurring 7-hydroxycoumarins as identified by mass spectroscopy, ESI-MS. In addition to antifungal effects, coumarins function as fluorescent whitening agents in Phormium fibres and play a role in the fibre’s photodegradation. Ultraviolet irradiation (350 – 400 nm) of the fibre resulted in a substantial loss of the blue fluorescence originating from a number of 7-hydroxycoumarins present, together with the formation of new fluorophores absorbing and emitting at longer wavelengths, which contribute to the photoyellowing of the fibre. The photolysis of two standard 7-hydroxycoumarins in aqueous solution was examined and two primary photoproducts were elucidated by ESI-MS: a photodimer containing a linking cyclobutane ring and a monomeric photooxidation product. The formation of at least some of the photoproducts is associated with the coumarin-sensitised generation of reactive oxygen species, hydrogen peroxide and superoxide. The fluorescence properties and photodegradation of Chinese handmade papers were also investigated. Papers manufactured by traditional methods were found to be more photostable than that produced from chemically-facilitated techniques.</p>


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